FDA NDC Directory · JSON-LD · Markdown

Furosemide

NDC 43063-849 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namefurosemide
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076796
Dosage form / routeTABLET · ORAL
Active ingredientsFUROSEMIDE (20 mg/1)
Marketing started20040326
Package count4

External sources

Source: openFDA. Public-domain (CC0).